Overview Join Precision for Medicine as a Clinical Project Manager/Senior CPM to lead end‑to‑end general oncology trials in a CRO environment. You will drive project delivery, manage cross‑functional teams, and maintain client relationships, budgets, and timelines from proposal through study completion. You’ll ensure quality and coordination across data management, safety, clinical, and biostatistics, partnering with sponsors and internal teams to deliver impactful cancer trials. This is a high‑energy, collaborative role with a clear impact on patients and science.
Compensaciones / Beneficioswork-life balancecollaborative team cultureopportunity for growthdynamic, high-energy environment ResponsabilidadesLead and independently manage clinical projects within budget and scopeServe as primary client contact and participate in proposals and client presentationsCoordinate with project team and senior management across Precision and sponsorsOversee all trial aspects across functional areas (data management, safety, clinical,
biostatistics)Prepare and review protocols, study documents, budgets, and site contractsProvide regular status updates and define delivery metrics and escalationsContribute to efficient trial execution as an active project team member Requisitos principalesDegree or life science qualification (or equivalent experience)Previous full-service/global PM experience in CROsExperience in oncology trialsGCP/ICH knowledge and clinical development process understandingWillingness to travel domestically and internationallyFluent English, strong presentation skillsProven computer and software skills (MS Office, MS Project, PowerPoint) and experience with CTMS, eTMF, EDC, IXRSProven ability to build positive internal and external relationshipsClinical terminology and trial activities understandingstrong interpersonal and organizational skillsexcellent client-facing communicationcross-functional collaborationCTMSeTMFEDC